Canonical Allele Identifier: PA267659
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120278
ClinVar RCV Id: RCV000106359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu183Leu
CA267658
NM_000277.3:c.547_548delinsTT